Recombinant Rat DLL1 Protein (His Tag)
Beta LifeScience
SKU/CAT #: BLPSN-1627
Recombinant Rat DLL1 Protein (His Tag)
Beta LifeScience
SKU/CAT #: BLPSN-1627
Collections: Other recombinant proteins, Recombinant proteins
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Product Overview
Tag | His |
Host Species | Rat |
Accession | G3V7W7 |
Background | Delta-like protein 1(DLL1), also known as Delta1, a single-pass type I membrane protein which contains one DSL domain and eight EGF-like domains, acts as a ligand for Notch receptors, and positively regulates T-cell development. DLL1 is proteolytically processed in a similar manner to the Notch receptor, and it has been speculated to participate in bidirectional signaling. The proteolytic processing of DLL1 helps achieve an asymmetry in Notch signaling in initially equivalent myogenic cells and helps sustain the balance between differentiation and self-renewal. Interactions between DLL1 and Notch in trans activate the Notch pathway, whereas DLL1 binding to Notch in cis inhibits Notch signaling. DLL1 undergoes proteolytic processing in its extracellular domain by ADAM1. It had been demonstrated that DLL1 represents a substrate for several other members of the ADAM family. In co-transfected cells, DLL1 is constitutively cleaved by ADAM12, and the N-terminal fragment of DLL1 is released to medium. ADAM12-mediated cleavage of DLL1 is cell density-dependent, takes place in cis orientation, and does not require the presence of the cytoplasmic domain of ADAM12. Full-length DLL1, but not its N- or C-terminal proteolytic fragment, co-immunoprecipitates with ADAM12. By using a Notch reporter construct, we show that DLL1 processing by ADAM12 increases Notch signaling in a cell-autonomous manner. Furthermore, ADAM9 and ADAM17 have the ability to process DLL1. In contrast, ADAM15 does not cleave DLL1, although the two proteins still co-immunoprecipitate with each other. During fetal development, DLL1 is an essential Notch ligand in the vascular endothelium of large arteries to activate Notch1 and maintain arterial identity. DLL1-Notch signaling was required for VEGF receptor expression in fetal arteries. |
Description | A DNA sequence encoding the rat DLL1 (EDL99825.1) extracellular domain (Met 1-Ser 534) was expressed, fused with a His tag at the C-terminus. |
Source | HEK293 |
Predicted N Terminal | Gln 18 |
AA Sequence | Met 1-Ser 534 |
Molecular Weight | The recombinant rat DLL1 comprises 746 a.a. and has a predicted molecular mass of 81.7 kDa. |
Purity | >65% as determined by SDS-PAGE |
Endotoxin | < 1.0 EU per μg of the protein as determined by the LAL method |
Bioactivity | 1. Measured by its ability to bind human NOTCH1 in a functional ELISA.2. Measured by the ability of the immobilized protein to enhance BMP2-induced alkaline phosphatase activity in C3H10T1/2 mouse embryonic fibroblast cells.The ED50- for this effect is typically 2-10 µg/mL in the presence of 500 ng/mL recombinant human BMP2. |
Formulation | Lyophilized from sterile PBS, 20% glycerol, pH 7.4. |
Stability | The recombinant proteins are stable for up to 1 year from date of receipt at -70°C. |
Usage | For Research Use Only |
Storage | Store the protein under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |